The treatment of Wegener's granulomatosis, one of the most common forms of systemic vasculitis, has changed substantially over the past two decades. The principal aims of therapy are to control the ...

Wegener's granulomatosis (newly renamed granulomatosis with polyangiitis [WG/GPA]) is a granulomatous autoimmune inflammatory disorder of unknown etiology that is associated with anti-neutrophil ...

This page lists all known medications that could potentially lead to 'Wegener's granulomatosis' as a side effect. It's important to note that mild side effects are quite common with medications. The ...

Azathioprine (Imuran) was used in combination with duazomycin A, a glutamine antagonist, for treatment of two patients with advanced Wegener's granulomatosis with renal involvement. Prolonged survival ...

Two patients with chronic Wegener's granulomatosis presented with worsening proptosis and visual acuity. Both patients had been maintained on long-term corticosteroids, which led to masking of the ...

Here, we summarize the clinical course of a 23-year-old man who had received a diagnosis of Wegener's granulomatosis at 14 years of age. Various immunosuppressive regimens, including high-dose ...

Wegener's granulomatosis is a systemic inflammatory disease with a broad range of clinical manifestations. The complete form is characterized by necrotizing granulomatous inflammation of the upper and ...

Wegener’s granulomatosis (WG) is a granulomatous disorder associated with systemic necrotizing vasculitis. Wegener’s granulomatosis predominantly involves the upper airways, lung and kidneys. The ...

This patient had a history of fleeting arthralgia, and he had an elevated erythrocyte sedimentation rate (83 [normal 1–13] mm/hr). A computed tomography scan of the paranasal sinuses (Figure 1) showed ...